Canonical Allele Identifier: CA393088387

Gene: HCN4

Linked Data

• MyVariant Identifiers: chr15:g.73615741C>A (hg19) ; chr15:g.73323400C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.73323400C>A , CM000677.2:g.73323400C>A	GRCh38
NC_000015.9:g.73615741C>A , CM000677.1:g.73615741C>A	GRCh37
NC_000015.8:g.71402794C>A	NCBI36
NG_009063.1:g.50865G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261917.4:c.2693G>T MANE Select	ENSP00000261917.3:p.Gly898Val
ENST00000261917.3:c.2693G>T	ENSP00000261917.3:p.Gly898Val
NM_005477.2:c.2693G>T	NP_005468.1:p.Gly898Val
XM_011521148.1:c.1475G>T	XP_011519450.1:p.Gly492Val
XM_011521148.2:c.1475G>T	XP_011519450.1:p.Gly492Val
NM_005477.3:c.2693G>T MANE Select	NP_005468.1:p.Gly898Val